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Susann Friedel

Research Profile

Disorders

Genes & Molecular Sequences

Physiology

Geographic Areas

Germany

Concepts & Ideas

Chemicals & Drugs

Procedures

Anatomy

Chromosomes, Human, Pair 5

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Publications

TOP 3
Benno Graf Schimmelmann; Susann Friedel; Thuy Trang Nguyen; S Sauer; C I Ganz Vogel; Kerstin Konrad; C Wilhelm; J Sinzig; Tobias Renner; Marcel Romanos; H Palmason; Astrid Dempfle; Susanne Walitza; Christine M Freitag; Jobst Meyer; Martin Linder; Helmut Schäfer; Andreas Warnke; Klaus-Peter Lesch; B Herpertz-Dahlman; Anke Hinney; Johannes Hebebrand
Exploring the genetic link between RLS and ADHD.
Carla I G Vogel; Brandon Greene; André Scherag; Timo D Müller; Susann Friedel; Harald Grallert; Iris M Heid; Thomas Illig; H-Erich Wichmann; Helmut Schäfer; Johannes Hebebrand; Anke Hinney
Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry.
O Albayrak; Susann Friedel; Benno Graf Schimmelmann; Anke Hinney; Johannes Hebebrand
Genetic aspects in attention-deficit/hyperactivity disorder.

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All Publications

2009: Benno Graf Schimmelmann; Susann Friedel; Thuy Trang Nguyen; S Sauer; C I Ganz Vogel; Kerstin Konrad; C Wilhelm; J Sinzig; Tobias Renner; Marcel Romanos; H Palmason; Astrid Dempfle; Susanne Walitza; Christine M Freitag; Jobst Meyer; Martin Linder; Helmut Schäfer; Andreas Warnke; Klaus-Peter Lesch; B Herpertz-Dahlman; Anke Hinney; Johannes Hebebrand
Exploring the genetic link between RLS and ADHD.
Journal of psychiatric research 2009;43(10):941-5.
2009: Carla I G Vogel; Brandon Greene; André Scherag; Timo D Müller; Susann Friedel; Harald Grallert; Iris M Heid; Thomas Illig; H-Erich Wichmann; Helmut Schäfer; Johannes Hebebrand; Anke Hinney
Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry.
BMC medical genetics 2009;10():14.
2008: O Albayrak; Susann Friedel; Benno Graf Schimmelmann; Anke Hinney; Johannes Hebebrand
Genetic aspects in attention-deficit/hyperactivity disorder.
Journal of neural transmission (Vienna, Austria : 1996) 2008;115(2):305-15.
2007: Naoe Okamura; Kenji Hashimoto; Masaomi Iyo; Eiji Shimizu; Astrid Dempfle; Susann Friedel; Rainer K Reinscheid
Gender-specific association of a functional coding polymorphism in the Neuropeptide S receptor gene with panic disorder but not with schizophrenia or attention-deficit/hyperactivity disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2007;31(7):1444-8.
2007: Susann Friedel; Kathrin Saar; S Sauer; Astrid Dempfle; Susanne Walitza; Tobias Renner; Marcel Romanos; Christine M Freitag; C Seitz; H Palmason; André Scherag; C Windemuth-Kieselbach; Benno Graf Schimmelmann; Christoph Wewetzer; J Meyer; Andreas Warnke; Klaus-Peter Lesch; R Reinhardt; Beate Herpertz-Dahlmann; Martin Linder; Anke Hinney; Helmut Remschmidt; Helmut Schäfer; Kerstin Konrad; N Hübner; Johannes Hebebrand
Association and linkage of allelic variants of the dopamine transporter gene in ADHD.
Molecular psychiatry 2007;12(10):923-33.
2007: Timo Dirk Müller; Kathrin Reichwald; Anne-Kathrin Wermter; Günter Brönner; Thuy Trang Nguyen; Susann Friedel; Kerstin Koberwitz; Stefan Engeli; Peter Lichtner; Thomas Meitinger; Helmut Schäfer; Johannes Hebebrand; Anke Hinney
No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents.
Molecular genetics and metabolism 2007;90(4):429-34.
2007: Anke Hinney; Thuy Trang Nguyen; André Scherag; Susann Friedel; Günter Brönner; Timo Dirk Müller; Harald Grallert; Thomas Illig; H-Erich Wichmann; Winfried Rief; Helmut Schäfer; Johannes Hebebrand
Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants.
PloS one 2007;2(12):e1361.
2007: Susann Friedel; Kathrin Reichwald; André Scherag; Harald Brumm; Anne-Kathrin Wermter; Hans-Rudolf Fries; Kerstin Koberwitz; Martin Wabitsch; Thomas Meitinger; Matthias Platzer; Heike Biebermann; Anke Hinney; Johannes Hebebrand
Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.
BMC genetics 2007;8():17.
2007: Benno Graf Schimmelmann; Susann Friedel; Astrid Dempfle; Andreas Warnke; Klaus-Peter Lesch; Susanne Walitza; Tobias Renner; Marcel Romanos; Beate Herpertz-Dahlmann; Martin Linder; Helmut Schäfer; C Seitz; H Palmason; Christine M Freitag; J Meyer; Kerstin Konrad; Anke Hinney; Johannes Hebebrand
No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD.
Journal of neural transmission (Vienna, Austria : 1996) 2007;114(4):523-6.
2007: Philip Heiser; Astrid Dempfle; Susann Friedel; Kerstin Konrad; Anke Hinney; H Kiefl; Susanne Walitza; Thomas Bettecken; Kathrin Saar; Martin Linder; Andreas Warnke; Beate Herpertz-Dahlmann; Helmut Schäfer; Helmut Remschmidt; Johannes Hebebrand
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample.
Journal of neural transmission (Vienna, Austria : 1996) 2007;114(4):513-21.
2006: Benno Graf Schimmelmann; Susann Friedel; Hanna Christiansen; Astrid Dempfle; Anke Hinney; Johannes Hebebrand
[Genetic findings in Attention-Deficit and Hyperactivity Disorder (ADHD)].
Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie 2006;34(6):425-33.
2006: Astrid Dempfle; Stefan A Wudy; Kathrin Saar; Sandra Hagemann; Susann Friedel; André Scherag; Lars D Berthold; Gerhard Alzen; Ludwig Gortner; Werner F Blum; Anke Hinney; Peter Nürnberg; Helmut Schäfer; Johannes Hebebrand
Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies.
Human molecular genetics 2006;15(18):2772-83.
2006: Philip Heiser; Monika Heinzel-Gutenbrunner; Joachim Frey; Judith Smidt; Justyna Grabarkiewicz; Susann Friedel; Wolfgang Kühnau; Jörg Schmidtke; Helmut Remschmidt; Johannes Hebebrand
Twin study on heritability of activity, attention, and impulsivity as assessed by objective measures.
Journal of attention disorders 2006;9(4):575-81.
2006: Johannes Hebebrand; Astrid Dempfle; Kathrin Saar; H Thiele; Beate Herpertz-Dahlmann; Martin Linder; H Kiefl; Helmut Remschmidt; U Hemminger; Andreas Warnke; U Knölker; Philip Heiser; Susann Friedel; Anke Hinney; Helmut Schäfer; Peter Nürnberg; Kerstin Konrad
A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs.
Molecular psychiatry 2006;11(2):196-205.
2005: Susanne Walitza; Tobias Renner; Astrid Dempfle; Kerstin Konrad; Christoph Wewetzer; Astrid Halbach; Beate Herpertz-Dahlmann; Helmut Remschmidt; Judith Smidt; Martin Linder; L Flierl; U Knölker; Susann Friedel; Helmut Schäfer; C Gross; Johannes Hebebrand; Andreas Warnke; Klaus-Peter Lesch
Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder.
Molecular psychiatry 2005;10(12):1126-32.
2005: Susann Friedel; F Fontenla Horro; Anne-Kathrin Wermter; Frank Geller; Astrid Dempfle; Kathrin Reichwald; Judith Smidt; Günter Brönner; Kerstin Konrad; Beate Herpertz-Dahlmann; Andreas Warnke; U Hemminger; Martin Linder; H Kiefl; Hanspeter Goldschmidt; Wolfgang Siegfried; Helmut Remschmidt; Anke Hinney; Johannes Hebebrand
Mutation screen of the brain derived neurotrophic factor gene (BDNF): identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;132B(1):96-9.
2004: Philip Heiser; Susann Friedel; Astrid Dempfle; Kerstin Konrad; Judith Smidt; Justyna Grabarkiewicz; Beate Herpertz-Dahlmann; Helmut Remschmidt; Johannes Hebebrand
Molecular genetic aspects of attention-deficit/hyperactivity disorder.
Neuroscience and biobehavioral reviews 2004;28(6):625-41.
2004: Anke Hinney; Susann Friedel; Helmut Remschmidt; Johannes Hebebrand
Genetic risk factors in eating disorders.
American journal of pharmacogenomics : genomics-related research in drug development and clinical practice 2004;4(4):209-23.
2004: Hai-Jun Wang; Frank Geller; Astrid Dempfle; Nadine Schäuble; Susann Friedel; Peter Lichtner; Francisco Fontenla-Horro; Stefan A Wudy; Sandra Hagemann; Ludwig Gortner; Klaus Huse; Helmut Remschmidt; Thomas Bettecken; Thomas Meitinger; Helmut Schäfer; Johannes Hebebrand; Anke Hinney
Ghrelin receptor gene: identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal stature.
The Journal of clinical endocrinology and metabolism 2004;89(1):157-62.
2003: Johannes Hebebrand; Susann Friedel; Nadine Schäuble; Frank Geller; Anke Hinney
Perspectives: molecular genetic research in human obesity.
Obesity reviews : an official journal of the International Association for the Study of Obesity 2003;4(3):139-46.
2003: Kathrin Saar; Frank Geller; Franz Rüschendorf; André Reis; Susann Friedel; Nadine Schäuble; Peter Nürnberg; Wolfgang Siegfried; Hans-Peter Goldschmidt; Helmut Schäfer; Andreas Ziegler; Helmut Remschmidt; Anke Hinney; Johannes Hebebrand
Genome scan for childhood and adolescent obesity in German families.
Pediatrics 2003;111(2):321-7.
2002: Susann Friedel; Benjamin Antwerpen; Anne Hoch; Constanze Vogel; Wolfgang Grassl; Frank Geller; Johannes Hebebrand; Anke Hinney
Glucose transporter 4 gene: association studies pertaining to alleles of two polymorphisms in extremely obese children and adolescents and in normal and underweight controls.
Annals of the New York Academy of Sciences 2002;967():554-7.